View genomic variant #0000001045

Chromosome 5
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.131705676C>G
Published as -
GERP 4.990
Segregation -
DB-ID SLC22A5_000055 See all 2 reported entries
MSCV MSCV_0001045
dbSNP ID rs72552722
Frequency -
Sources ; clinvar; ensembl;
Reference 11715001
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts

3 entries on 1 page. Showing entries 1 - 3.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
SLC22A5 00001145 NM_003060.3 0000001045 +/+ - 1/10 c.12C>G p.(Tyr4*) - stop_gained - -
SLC22A5 00001144 XM_005272055.1 0000001045 +/+ - 1/10 c.12C>G p.(Tyr4*) - stop_gained - -
SLC22A5 00001146 XM_005272056.1 0000001045 +/+ - - c.-389C>G p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000022293; RCV003398556;
Chromosome 5:131705676..131705676
Allele frequencies from ExAC 0.00002
ClinVar Allele ID 36681
Disease database name and identifier .|MONDO:MONDO:0008919, MedGen:C0342788, OMIM:212140, Orphanet:158
ClinVar preferred disease name SLC22A5-related condition|Renal carnitine transport defect
HGVS variant names NC 000005.9:g.131705676C>G
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic/Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA342604|OMIM:603377.0024
Gene symbol:Gene id. SLC22A5:6584
Molecular consequence SO:0001587|nonsense
Allele origin germline
dbSNP ID 72552722
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000665371;
Chromosome 5:131705677..131705677
ClinVar Allele ID 543578
Disease database name and identifier MONDO:MONDO:0008919, MedGen:C0342788, OMIM:212140, Orphanet:158
ClinVar preferred disease name Renal carnitine transport defect
HGVS variant names NC 000005.9:g.131705677del
ClinVar review status criteria provided, single submitter
Clinical Significance Likely pathogenic
Variant type Deletion
Sequence Ontology for variant type SO:0000159
Gene symbol:Gene id. SLC22A5:6584
Molecular consequence SO:0001589|frameshift variant
Allele origin unknown
dbSNP ID 1554085892
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

None